{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T02:09:52Z","timestamp":1767665392488},"reference-count":34,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2014,1,31]],"date-time":"2014-01-31T00:00:00Z","timestamp":1391126400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cathet Cardio Intervent"],"published-print":{"date-parts":[[2014,5]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>The efficacy and safety of primary stenting for superficial femoral artery (SFA) disease have been benchmarked against historically derived performance goals. However, contemporary evidence evaluating SFA stenting is accumulating. The objective of this systematic review and meta\u2010analysis was to quantitatively assess outcomes after primary SFA stenting with nitinol stents in contemporary practice, to compare these rates with commonly used efficacy and safety goals, and to discuss the clinical and regulatory implications of these findings.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods and Results<\/jats:title><jats:p>We searched MEDLINE, the US Food and Drug Administration (FDA) website, reference lists of qualifying articles, and conference proceedings until October 2012. Studies prospectively assessing primary nitinol stenting for diseased SFA were sought. Data from 11 prospective clinical trials were included. The twelve\u2010month primary patency (PP) rate was reported in five trials. The meta\u2010analytic 12\u2010month PP rate was 71.6% (95% confidence interval [CI] 66.4\u201376.7%). The meta\u2010analytic rate of 30\u2010day freedom from a composite of death, target limb amputation, and reintervention was 99.9% (95% CI 100.0\u201390.0%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Contemporary nitinol\u2010based bare\u2010metal stents performed well in controlled settings. Occurrence of the 1\u2010month composite safety endpoint was extremely uncommon. \u00a9 2013 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ccd.25179","type":"journal-article","created":{"date-parts":[[2013,9,2]],"date-time":"2013-09-02T05:28:34Z","timestamp":1378099714000},"page":"975-983","source":"Crossref","is-referenced-by-count":21,"title":["Safety and efficacy metrics for primary nitinol stenting in femoropopliteal occlusive disease: A meta\u2010analysis and critical examination of current methodologies"],"prefix":"10.1002","volume":"83","author":[{"given":"Moshe","family":"Vardi","sequence":"first","affiliation":[{"name":"Harvard Clinical Research Institute Boston Massachusetts"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Victor","family":"Novack","sequence":"additional","affiliation":[{"name":"Soroka Clinical Research Center Beer Sheva Israel"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael 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